FDA NDC Directory · JSON-LD · Markdown

Omeprazole

NDC 71335-9609 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA075757
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (20 mg/1)
Marketing started20190701
Package count10

External sources

Source: openFDA. Public-domain (CC0).